US4855412A - Diaminopyridine azo dyes having acyloxy radicals substituted on the diaminopyridine - Google Patents

Diaminopyridine azo dyes having acyloxy radicals substituted on the diaminopyridine Download PDF

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US4855412A
US4855412A US07/042,243 US4224387A US4855412A US 4855412 A US4855412 A US 4855412A US 4224387 A US4224387 A US 4224387A US 4855412 A US4855412 A US 4855412A
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Johannes Dehnert
Gunther Lamm
Hermann Loeffler
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BASF SE
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    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B29/00Monoazo dyes prepared by diazotising and coupling
    • C09B29/0025Monoazo dyes prepared by diazotising and coupling from diazotized amino heterocyclic compounds
    • C09B29/0074Monoazo dyes prepared by diazotising and coupling from diazotized amino heterocyclic compounds the heterocyclic ring containing nitrogen and sulfur as heteroatoms
    • C09B29/0077Monoazo dyes prepared by diazotising and coupling from diazotized amino heterocyclic compounds the heterocyclic ring containing nitrogen and sulfur as heteroatoms containing a five-membered heterocyclic ring with one nitrogen and one sulfur as heteroatoms
    • C09B29/0085Thiazoles or condensed thiazoles
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B29/00Monoazo dyes prepared by diazotising and coupling
    • C09B29/0025Monoazo dyes prepared by diazotising and coupling from diazotized amino heterocyclic compounds
    • C09B29/0059Monoazo dyes prepared by diazotising and coupling from diazotized amino heterocyclic compounds the heterocyclic ring containing only sulfur as heteroatom
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B29/00Monoazo dyes prepared by diazotising and coupling
    • C09B29/0025Monoazo dyes prepared by diazotising and coupling from diazotized amino heterocyclic compounds
    • C09B29/0074Monoazo dyes prepared by diazotising and coupling from diazotized amino heterocyclic compounds the heterocyclic ring containing nitrogen and sulfur as heteroatoms
    • C09B29/0077Monoazo dyes prepared by diazotising and coupling from diazotized amino heterocyclic compounds the heterocyclic ring containing nitrogen and sulfur as heteroatoms containing a five-membered heterocyclic ring with one nitrogen and one sulfur as heteroatoms
    • C09B29/0081Isothiazoles or condensed isothiazoles
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B29/00Monoazo dyes prepared by diazotising and coupling
    • C09B29/34Monoazo dyes prepared by diazotising and coupling from other coupling components
    • C09B29/36Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds
    • C09B29/3604Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds containing only a nitrogen as heteroatom
    • C09B29/3617Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds containing only a nitrogen as heteroatom containing a six-membered heterocyclic with only one nitrogen as heteroatom
    • C09B29/3621Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds containing only a nitrogen as heteroatom containing a six-membered heterocyclic with only one nitrogen as heteroatom from a pyridine ring
    • C09B29/3639Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds containing only a nitrogen as heteroatom containing a six-membered heterocyclic with only one nitrogen as heteroatom from a pyridine ring from a pyridine ring containing one or more amino groups
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S534/00Organic compounds -- part of the class 532-570 series
    • Y10S534/02Azo compounds containing chains of eight or more carbon atoms not provided for elsewhere in this class

Abstract

Compounds of the general formula ##STR1## where D is a radical of the formula ##STR2## and one of the two radicals L1 and L2 is unsubstituted amino and the other the radical ##STR3## where R1 is hydrogen, C1 -C4 -alkyl, C1 -C4 -alkoxy-C2 -C4 -alkyl or C1 -C8 -acyloxy-C2 -C4 -alkyl,
R2 is C2 -C10 -alkylene or C2 -C10 -alkylene is interrupted by oxygen,
T is C1 -C8 -alkanoyl which is unsubstituted or is substituted by chlorine or methoxy,
B1 is C1 -C4 -alkyl or benzyl or phenyl, which are each unsubstituted or are each substituted by methyl, methoxy or chlorine,
B2 is B1, hydrogen, halogen, cyano or C1 -C5 -alkoxycarbonyl,
X1 is hydrogen, nitro, cyano, C1 -C9 -alkoxycarbonyl, C1 -C9 -mono- or -dialkylaminocarbonyl, trifluoromethyl, methylsulfonyl or ethylsulfonyl,
X2 is nitro or C1 -C5 -alkoxycarbonyl,
X3 is X2, cyano or formyl,
Y is hydrogen, chlorine, bromine, methyl, methoxy or ethoxy and
Z is hydrogen, chlorine, bromine, cyano or C1 -C9 -alkoxycarbonyl which is unsubstituted or is substituted by C1 -C4 -alkoxy, and one or more of the substituents X1, Y and Z is different from hydrogen, are disclosed.
The dyes of the present invention may be used in dyeing synthetic polyester.

Description

The present invention relates to compounds of the formula I ##STR4## where D is a radical of the formula ##STR5## one of the two radicals L1 and L2 is unsubstituted amino and the other the radical ##STR6## where R1 is hydrogen, C1 -C4 -alkyl, C1 -C4 -alkoxy-C2 -C4 -alkyl or C1 -C8 -acyloxy-C2 -C4 -alkyl,

R2 is C2 -C10 -alkylene which may be interrupted by oxygen,

T is hydrogen or C1 -C8 -alkanoyl which may be substituted by chlorine or methoxy,

B1 is C1 -C4 -alkyl or benzyl or phenyl, which may each be substituted by methyl, methoxy or chlorine,

B2 is B1, hydrogen, halogen, cyano or C1 -C5 -alkoxycarbonyl,

X1 is hydrogen, nitro, cyano, C1 -C9 -alkoxycarbonyl, C1 -C9 -mono- or -dialkylaminocarbonyl, trifluoromethyl, methylsulfonyl or ethylsulfonyl,

X2 is nitro or C1 -C5 -alkoxycarbonyl,

X3 is X2, cyano or formyl,

Y is hydrogen, chlorine, bromine, methyl, methoxy or ethoxy and

Z is hydrogen, chlorine, bromine, cyano or C1 -C9 -alkoxycarbonyl which may be substituted by C1 -C4 -alkoxy, and one or more of the substituents X1, Y and Z is different from hydrogen.

R1, B1 and B2 in the formula I are for example methyl, ethyl, propyl, isopropyl, butyl, isobutyl or sec-butyl.

R1 can further be 2-methoxyethyl, 2-ethoxyethyl, 2-methoxypropyl, 3-methoxypropyl, 4-methoxybutyl, 2-formyloxyethyl, 2-acetyloxyethyl, 2-propionyloxyethyl, 2-isobutyryloxyethyl, 2-hexanoyloxyethyl, 2-octanoyloxyethyl, 2-(2'-ethylhexanoyloxy)ethyl, 2- or 3-formyloxypropyl, 2- or 3-acetyloxypropyl, 2- or 3-propionyloxypropyl, 2- or 3-isobutyryloxypropyl, 2- or 3-hexanoyloxypropyl, 2- or 3-octanoyloxypropyl, 2- or 3-(2'-ethylhexanoyloxy)propyl, 4-acetyloxybutyl or 4-(2'-ethylhexanoyloxy)butyl.

B1 and B2 can further be benzyl, 2-methylbenzyl, 4-methylbenzyl, 2-methoxybenzyl, 4-methoxybenzyl, 2,4-dimethoxybenzyl, 2-chlorobenzyl, 4-chlorobenzyl, phenyl, 2-methylphenyl, 4-methylphenyl, 2,4-dimethylphenyl, 2-methoxyphenyl, 4-methoxyphenyl, 2-chlorophenyl, 4-chlorophenyl or 2,6-dichlorophenyl.

Alkylene radicals R2 are for example: ##STR7##

T in the formula I is for example formyl, acetyl, propionyl, isobutyryl, pentanoyl, 2,2-dimethylpropanoyl, hexanoyl, heptanoyl, octanoyl, 2-ethylhexanoyl, chloroacetyl or methoxyacetyl.

B2 in the formula I is for example chlorine or bromine.

B2, like X1, X2, X3 and Z, can also be for example methoxycarbonyl, ethoxycarbonyl, propoxycarbonyl, isopropoxycarbonyl, butoxycarbonyl, isobutoxycarbonyl, sec-butoxycarbonyl or pentyloxycarbonyl.

X1 and Z can also be for example hexyloxycarbonyl, heptyloxycarbonyl, octyloxycarbonyl, 2-ethylhexyloxycarbonyl or nonyloxycarbonyl.

X1 can also be for example methylaminocarbonyl, ethylaminocarbonyl, propylaminocarbonyl, isopropylaminocarbonyl, butylaminocarbonyl, isobutylaminocarbonyl, sec-butylaminocarbonyl, pentylaminocarbonyl, hexylaminocarbonyl, heptylaminocarbonyl, octylaminocarbonyl, 2-ethylhexylaminocarbonyl, nonylaminocarbonyl, dimethylaminocarbonyl, or diethylaminocarbonyl.

Z can also be for example 2-methoxyethoxycarbonyl, 2-ethoxyethoxycarbonyl or 3-methoxypropoxycarbonyl.

To prepare a compound according to the invention of the formula I, a coupling component of the formula II ##STR8## where one of the radicals L3 and L4 is unsubstituted amino and the other the radical ##STR9## where R1 and R2 have the abovementioned meanings, can be treated in an excess of an organic monocarboxylic acid of the formula T2 --OH, where T2 is C1 -C8 -alkanoyl which may be substituted by chlorine or methoxy, in the presence of a mineral acid or of an organic sulfonic acid at from 0° to 120° C., preferably from 20° to 60° C., with or without elimination of the water of reaction, and the acylation product is subsequently coupled in a conventional manner with a diazonium salt derived from an amine of the formula D--NH2, where D has the abovementioned meanings, to give a dye of the formula I.

The acylation in the above sequence can advantageously be combined with the preparation of the hydroxyalkylaminopyridine, thereby saving the intermediate isolate thereof and minimizing the use of acylating agent.

Similarly, it is alo possible to acylate an azo dye of the formula III ##STR10## where D, L3 and L4 each have the abovementioned meanings, to give a novel dye of the formula I.

The degree of acylation can be controlled via the amount of mineral or sulfonic acid and the water content of the reaction mixture and, in the absence of water, is 100%.

Complete acylation is usually not necessary for the resulting dye to have optimal dyeing properties. Frequently, it is precisely the choice of degree of acylation which makes it possible to optimize diverging dyeing and fastness properties such as exhaustion, temperature dependence, buildup and fastness to dry heat setting.

The methods described in DE-A Nos. 2,156,545 and 2,251,702 for acylating aminopyridines using acid anhydrides or halides, if applied to a compound of the formula II, also block the unsubstituted amino group. The corresponding acylamino compounds, however, are no longer couplable, so that acylated dyes of the formula I are obtainable in this way only in considerably reduced yields, if at all.

The novel dyes of the formula I are highly suitable for dyeing synthetic polyesters, giving excellent dyeings of very good light fastness, wash fastness and heat setting fastness.

Of particular importance are dyes of the formula I where D is a radical of the formula ##STR11## one of the two radicals L1 and L2 is an unsubstituted amino group and the other is --NH--R3 --O--T1, where

R3 is (CH2)2 O(CH2)2, (CH2)3 O(CH2)3 or (CH2)3 O(CH2)4,

T1 is hydrogen or C1 -C4 -alkanoyl,

X4 is nitro, cyano, methylsulfonyl or ethylsulfonyl,

Y2 is hydrogen, chlorine or bromine,

Z2 is hydrogen, cyano or C1 -C5 -alkoxycarbonyl,

B3 is C1 -C3 -alkyl, benzyl or phenyl and

R4 is methyl or ethyl.

Very particular preference is given to mixtures of the novel compounds of the formula I where on the one hand one of the two radicals L1 and L2 is an unsubstituted amino group and the other is --NH--R3 --OH and on the other hand one of the two radicals L1 and L2 is unsubstituted amino and the other is NH--R3 --O--T3, where R3 has in each case the abovementioned meanings and T3 is C1 -C4 -alkanoyl.

These mixtures contain for example individual components which conform to the formula IV ##STR12## where D has the abovementioned meanings. In the individual components IVa to IVd, the radicals A1 and A2 have the following meanings:

______________________________________IVa:    A.sup.1 = hydrogen                 IVb:     A.sup.1 = R.sup.3 --OH   A.sup.2 = R.sup.3 --OH A.sup.2 = hydrogenIVc:    A.sup.1 = hydrogen                 IVd:     A.sup.1 = R.sup.3 --OT.sup.3   A.sup.2 = R.sup.3 --OT.sup.3                          A.sup.2 = hydrogen.______________________________________

These mixtures are formed for example on reacting 2,6-dichloro-3-cyano-4-methylpyridine first with ammonia and then with an appropriate alkanolamine, thereafter acylating and subsequently coupling. As stated above, the degree of acylation, ie. the molar ratio IVa:IVc and IVb:IVd, depends on the reaction conditions.

The isomer ratios IVa:IVb and IVc:IVd are in addition dependent on the coupling activity of the diazo component and the amount of coupling component used in relation thereto and can vary within wide limits. Preference is given to an isomer ratio of IVa:IVb and IVc:IVd of from 3:2 to 3:1.

Further details of the preparation can be found in the Examples, where parts and percentages are by weight, unless otherwise stated.

The λmax values were always measured in acetone.

EXAMPLE 1

13.8 parts of 4-nitroaniline were dissolved in 200 parts by volume of hot water using 30 parts by volume of 30% strength hydrochloric acid. The still warm solution was poured onto 300 parts of ice, and 30 parts by volume of 3.33N sodium nitrite solution were rapidly added. The mixture was stirred for about 15 minutes in the presence of an excess of nitrous acid, and this excess was then destroyed with a little sulfamic acid. The resulting diazonium salt solution was then added to the solution of the coupling component, which was prepared as follows:

A mixture of 17 parts of 2-chloro-3-cyano-4-methyl-6-aminopyridine, 20 parts by volume of isobutanol, 18 parts of 3-aminopropyl 4-hydroxybutyl ether and 8 parts of sodium carbonate was heated for 5 hours with thorough stirring at 145°/150° C. using a descending condenser until a thin layer chromatogram indicated complete conversion. After cooling down to about 100° C., 35 parts of acetic acid were then added dropwise, followed at 35°/40° C. with continued gentle cooling by 15 parts of 96% strength sulfuric acid. After 3 hours of stirring under a pressure of 45 mm Hg, 96% of the hydroxy compound had been acetylated.

To obtain coupling, the reaction mixture was diluted with 300 parts of ice and 100 parts by volume of water. By gradual addition of 100 parts by volume of saturated sodium acetate solution (reaction mixture pH: about 2) and stirring for about an hour at about +5° C., the diazonium salt was made to react. Thereafter the reaction mixture was filtered off with suction, and the filter cake was washed until neutral and dried at 80° C.

The resulting brownish red powder corresponds to about 92% to the isomer mixture of the formula ##STR13## and still contains about 8% of unacetylated hydroxy compounds.

On application to PES fabric by the high-temperature method, this powder produced a very strong dyeing with complete exhaustion of the dyebath at as low a temperature as 125°/130° C. The dyeing exhibited excellent allround fastness.

EXAMPLE 2

17.3 parts of 2-chloro-4-nitroaniline were stirred together with 40 parts by volume of 30% strength hydrochloric acid for one hour in 120 parts of water. Water and ice were added to bring the volume to 500 parts and the temperature to 10° C., and 30 parts by volume of 3.33N sodium nitrite solution were then introduced underneath the surface. After two hours' stirring at 10° C. with excess acid present, 250 parts of ice were added to the diazonium salt solution. Then the solution of the coupling component, prepared as described in Example 1 but acylated with 40 parts of propionic acid instead of acetic acid, was added. (The water content of the acetylation mixture was 10%.)

After two hours of stirring at from 5° to 10° C., the diazonium salt had been consumed. This was followed by cold filtration with suction, washing of the filter cake until neutral and drying at 80° C.

The resulting reddish brown powder corresponds to about 75% to the isomer mixture ##STR14## and still contains about 25% of unacylated hydroxy isomer.

Applied to PES by the high-temperature method at 125°/130° C., the dye gave very strong reddish orange dyeings of very good allround fastness.

EXAMPLE 3

16.3 parts of 2-cyano-4-nitroanilline were suspended at 10°/15° C. in 150 parts by volume of glacial acetic acid and 50 parts by volume of propionic acid by stirring. 31.5 parts of 40% strength nitrosylsulfuric acid were added dropwise, which was followed by two hours of stirring at 10°/15° C. until solution was complete. Said solution was added to a coupling component solution prepared from 250 parts of ice and, after acylation with 40 parts of isobutyric acid, the component of Example 1. The acylation mixture contained 2% of water.

The coupling reaction was complete within a short time. The dye was filtered off with suction, washed until neutral and dryed at 80° C.

The red powder obtained contained about 85% of a mixture of the acyl isomers ##STR15## and dyed PES in yellowish red shades of very high fastness.

The procedures of Examples 1, 2 and 3 can be used, if desired with slight variation in concentration, temperature and solvent, to obtain the dyes described in the Tables below, which give similar results in terms of color and fastness.

The dyes which are characterized hereinafter in terms of substituents are indicated in each case only in the form of the main isomer. However, these dyes always exist in the form of the isomer mixtures formed with complete or incomplete acylation in the method of preparation described.

__________________________________________________________________________ ##STR16##Example                                            λ maxNo.  X.sup.1      Y     Z         R.sup.1 R.sup.2OT       nm__________________________________________________________________________4    4-NO.sub.2      H     H         H       C.sub.3 H.sub.6OC.sub.4 H.sub.8OCOC.sub                              .2 H.sub.5      4655    4-NO.sub.2      2-Cl  H         H       C.sub.3 H.sub.6OC.sub.4 H.sub.8OCOCH.su                              b.3             4836    4-NO.sub.2      H     2-CN      H       C.sub.3 H.sub.6OC.sub.4 H.sub.8OCOC.sub                              .2 H.sub.5      5007    4-NO.sub.2      2-Cl  6-CN      H       C.sub.3 H.sub.6OC.sub.4 H.sub.8OCOCH.su                              b.3             5078    4-NO.sub.2      2-Cl  6-CN      H       C.sub.3 H.sub.6OC.sub.4 H.sub.8OCOH                                              5079    4-NO.sub.2      2-Cl  6-CN      H       C.sub.2 H.sub. 4OC.sub.2 H.sub.4OCOCH.s                              ub.3            50610   4-SO.sub.2 CH.sub.3      2-Cl  H         H       C.sub.3 H.sub.6OC.sub.4 H.sub.8OCOCH.su                              b.3             45311   4-NO.sub.2      H     2-COOC.sub.2 H.sub.4 OCH.sub.3                      H       C.sub.3 H.sub.6OCOC.sub.2 H.sub.5                                              48012   4-CN  2-Cl  H         H       C.sub.3 H.sub.6OC.sub.4 H.sub.8OCOCH.su                              b.3             45713   4-Cl  H     2-CN      H       C.sub.3 H.sub.6OC.sub.4 H.sub.8OCOCH.su                              b.3             45314   4-NO.sub.2      H     H         C.sub.4 H.sub.9                              C.sub.2 H.sub.4OCOCH.sub.3                                              473.515   4-NO.sub.2      H     H         C.sub.2 H.sub.4 OCH.sub.3                              C.sub.2 H.sub.4OCOC.sub.2 H.sub.5                                              47316   4-NO.sub.2      2-Cl  H         C.sub.2 H.sub.4 OCOC.sub.2 H.sub.5                              C.sub.2 H.sub.4OCOC.sub.2 H.sub.5                                              49117   4-NO.sub.2      H     6-CN      C.sub.2 H.sub.5                              C.sub.2 H.sub.4OCOCH(CH.sub.3).sub.2                                              50818   4-NO.sub.2      H     H         H                               ##STR17##      46319   4-NO.sub.2      2-Cl  H         H                               ##STR18##      48420   4-NO.sub.2      2-Cl  H         H       C.sub.6 H.sub.12OCOCH.sub.3                                              48421   2-CN  H     H         H       C.sub.3 H.sub.6OC.sub.4 H.sub.8OCOCH.su                              b.3             44022   4-NO.sub.2      2-SO.sub.2 C.sub.2 H.sub.5            H         H       C.sub.3 H.sub.6OC.sub.4 H.sub.8OCOCH.su                              b.3             50123   4-NO.sub.2      2-Cl  H         H                               ##STR19##      48224   4-NO.sub.2      H     6-CN      H       C.sub.3 H.sub.6OCOCH.sub.2 OCH.sub.3                                              50125   4-NO.sub.2      H     6-CN      C.sub.4 H.sub.9                              C.sub.2 H.sub.4OCOC.sub.2 H.sub.5                                              508.526   4-NO.sub.2      2-Cl  6-CN      C.sub.2 H.sub.4 OCH.sub.3                              C.sub.2 H.sub.4OCOC.sub.2 H.sub.5                                              51427   4-NO.sub.2      H     H         H                               ##STR20##      46428   4-NO.sub.2      H     H         H                               ##STR21##      46329   4-NO.sub.2      2-Cl  H         H                               ##STR22##      482__________________________________________________________________________ ##STR23##Example                                       λ maxNo.     R        R.sup.1   R.sup.2OT          nm__________________________________________________________________________30      CH.sub.3 H         C.sub.3 H.sub.6OC.sub.4 H.sub.8OCOCH.sub.3                                         516.531      CH.sub.3 H         C.sub.3 H.sub.6OC.sub.4 H.sub.8OCOC.sub.2                      H.sub.5            516.532      CH.sub.3 H         C.sub.3 H.sub.6OC.sub.4 H.sub.8OCOCH(CH.sub.3).                      sub.2              516.533      CH.sub.3 H                       ##STR24##         51834      C.sub.2 H.sub.5            H         C.sub.3 H.sub.6OC.sub.4 H.sub.8OCOC.sub.2                      H.sub.5            516.535      C.sub.4 H.sub.9            H         C.sub.3 H.sub.6OC.sub.4 H.sub.8OCOCH.sub.3                                         51736      CH.sub.3 C.sub.4 H.sub.9                      C.sub.2 H.sub.4OCOCH.sub.3                                         52537      CH.sub.3 C.sub.2 H.sub.4 OCH.sub.3                      C.sub.2 H.sub.4OCOC.sub.2 H.sub.5                                         52438      C.sub.4 H.sub.9            C.sub.4 H.sub.9                      C.sub.2 H.sub.4OCHO                                         52539      CH.sub.3 H                       ##STR25##         51640      CH.sub.3 H                       ##STR26##         515__________________________________________________________________________ ##STR27##Example                                       λ maxNo.     R        R.sup.1   R.sup. 2OT         nm.sup.1__________________________________________________________________________41      CH.sub.3 H         C.sub.3 H.sub.6OC.sub.4 H.sub.8OCOCH(CH.sub.3).                      sub.2              50642      CH.sub.3 H                       ##STR28##         50743      CH(CH.sub.3).sub.2            H         C.sub.3 H.sub.6OC.sub.4 H.sub.8OCOCH.sub.3                                         50644    ##STR29##            H         C.sub.3 H.sub.6OC.sub.4 H.sub.8OCOCH.sub.3                                         50945    ##STR30##            H         C.sub.3 H.sub.6OCOC.sub.2 H.sub.5                                         51046      CH.sub.3 C.sub.4 H.sub.9                      C.sub.2 H.sub.4OCOCH.sub.3                                         52247    ##STR31##            C.sub.4 H.sub.9                      C.sub.2 H.sub.4OCOCH.sub.3                                         52548    ##STR32##            C.sub.4 H.sub.9                       ##STR33##         510__________________________________________________________________________ ##STR34##Example                                       λ maxNo.  B.sup.2    X.sup.3                 R.sup.1 R.sup.2OT       nm__________________________________________________________________________49 ##STR35## CN    H       C.sub.3 H.sub.6OC.sub.4 H.sub.8OCOCH.sub.3                                         50050 ##STR36## CN    H       CH(CH.sub.3)C.sub.2 H.sub.4OCOCH.sub.3                                         50151 ##STR37## CN    H       C.sub.3 H.sub.6OCOC.sub.2 H.sub.5                                         50152   COOC.sub.2 H.sub.5           COOC.sub.2 H.sub.5                 H       C.sub.3 H.sub.6OC.sub.4 H.sub.8OCOC.sub.2                         H.sub.5         49353   COOC.sub.2 H.sub.5           COOC.sub.2 H.sub.5                 H                          ##STR38##      49454 ##STR39## CN    C.sub.2 H.sub.5                         C.sub.2 H.sub.4O COCH.sub.3                                         50855   COOC.sub.2 H.sub.5           COOC.sub.2 H.sub.5                 C.sub.4 H.sub.9                         C.sub.2 H.sub.4OCOCH.sub.3                                         501.556   COOC.sub.2 H.sub.5           CN    C.sub.4 H.sub.9                         C.sub.2 H.sub.4OCOCH.sub.3                                         508.557   COOC.sub.2 H.sub.5           CN    H                          ##STR40##      50058   H          NO.sub.2                 H                          ##STR41##      51859   Cl         CHO   H                          ##STR42##      51760   CH.sub.3   COOC.sub.2 H.sub.5                 H                          ##STR43##      49361   CH.sub.3   COOCH.sub.3                 H                          ##STR44##      49762   CN         COOCH.sub.3                 H                          ##STR45##      508__________________________________________________________________________ .sup. 1 in 9:1 DMF/acetic acid

Claims (2)

We claim:
1. A compound of the formula: ##STR46## where D is a radical of the formula ##STR47## one of the two radicals L1 and L2 is unsubstituted amino and the other radical is ##STR48## where R1 is hydrogen, C1 -C4 -alkyl, C1 -C4 -alkoxy-C2 -C4 -alkyl or C1 -C8 -alkanoyloxy-C2 -C4 -alkyl,
R2 is C2 -C10 -alkylene or C2 -C10 -alkylene which is interrupted by oxygen,
T is C1 -C8 -alkanoyl which is unsubstituted or is substituted by chlorine or methoxy,
B1 is C1 -C4 -alkyl or benzyl or phenyl, which are each unsubstituted or are each substituted by methyl, methoxy or chlorine,
B2 is B1, hydrogen, halogen, cyano or C1 -C5 -alkoxycarbonyl,
X1 is hydrogen, nitro, cyano, C1 -C9 -alkoxycarbonyl, C1 -C9 -mono- or -dialkylaminocarbonyl, trifluoromethyl, methylsulfonyl or ethylsulfonyl,
X2 is nitro or C1 -C5 -alkoxycarbonyl,
X3 is X2, cyano or formyl,
Y is hydrogen, chlorine, bromine, methyl, methoxy or ethoxy and
Z is hydrogen, chlorine, bromine, cyano or C1 -C9 -alkoxycarbonyl which is unsubstituted or is substituted by C1 -C4 -alkoxy, and one or more of the substituents X1, Y and Z is different from hydrogen.
2. A compound as claimed in claim 1, wherein
D is a radical of the formula ##STR49## one of the two radicals L1 and L2 is unsubstituted amino and the other is --NH--R3 --O--T1, where
R3 is (CH2)--O--(CH2)2, (CH2)3 O(CH2)3 or (CH2)3 O(CH2)4,
T1 is C1 -C4 -alkanoyl,
X4 is nitro, cyano, methylsulfonyl or ethylsulfonyl,
Y2 is hydrogen, chlorine or bromine,
Z2 is hydrogen, cyano or C1 -C5 -alkoxycarbonyl,
B3 is C1 -C3 -alkyl, benzyl or phenyl and
R4 is methyl or ethyl.
US07/042,243 1986-05-03 1987-04-24 Diaminopyridine azo dyes having acyloxy radicals substituted on the diaminopyridine Expired - Lifetime US4855412A (en)

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US5144240A (en) * 1985-08-14 1992-09-01 Picker International, Inc. Nmr spectroscopy and imaging coil
US5278294A (en) * 1991-05-28 1994-01-11 Hoechst Mitsubishi Kasei Co., Ltd. Monoazo dye having diaminopyridine derivatives
US5330543A (en) * 1991-11-23 1994-07-19 Basf Aktiengesellschaft Thiopheneazo dyes with a coupling component of the diaminopyridine series
US5352774A (en) * 1985-05-14 1994-10-04 Sandoz Ag Dyes containing thiophene radicals
US5403363A (en) * 1992-12-07 1995-04-04 Basf Aktiengesellschaft Dye mixtures containing azo dyes having a coupling component from the diaminopyridine series
US5602238A (en) * 1994-08-29 1997-02-11 Ciba-Geigy Corporation Azothiophene dyes containing a 2,4,6-triamino-3-cyanopyridine coupling component
GB2335924A (en) * 1998-03-31 1999-10-06 Zeneca Ltd Dyes and ink jet inks based on 5-([N-substituted-aminoaryl]azo)-4-cyanoisothiazole derivatives
US20050261395A1 (en) * 2002-01-30 2005-11-24 Fuji Photo Film Co., Ltd. Ink composition and inkjet recording method
US20070231204A1 (en) * 2006-03-31 2007-10-04 Searete Llc, A Limited Liability Corporation Of The State Of Delaware Surveying sterilizer methods and systems
US20070286398A1 (en) * 2006-06-07 2007-12-13 Venkatesan Ramamoorthy Voice Recognition Dialing For Alphabetic Phone Numbers
US8114342B2 (en) 2006-03-31 2012-02-14 The Invention Science Fund I, Llc Methods and systems for monitoring sterilization status
US8277724B2 (en) 2006-03-31 2012-10-02 The Invention Science Fund I, Llc Sterilization methods and systems
US8758679B2 (en) 2006-03-31 2014-06-24 The Invention Science Fund I, Llc Surveying sterilizer methods and systems
US8932535B2 (en) 2006-03-31 2015-01-13 The Invention Science Fund I, Llc Surveying sterilizer methods and systems
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DE3528759A1 (en) * 1985-08-10 1987-02-19 Basf Ag heterocyclic azo dyes
DE3738374A1 (en) * 1987-11-12 1989-05-24 Basf Ag Thien-3-ylazofarbstoffe and their use
DE3938093A1 (en) * 1989-11-16 1991-05-23 Basf Ag thiazole

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US29640A (en) * 1860-08-14 Improvement in automatic rakes for harvesters
US4042578A (en) * 1972-03-10 1977-08-16 Badische Anilin- & Soda-Fabrik Aktiengesellschaft Azo dyes having 2,6-diaminopyridine derivatives as coupling components
US3980659A (en) * 1972-06-22 1976-09-14 Cassella Farbwerke Mainkur Aktiengesellschaft Certain 6-amino-4-hydrocarbyl-nicotinamides

Cited By (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5352774A (en) * 1985-05-14 1994-10-04 Sandoz Ag Dyes containing thiophene radicals
US5144240A (en) * 1985-08-14 1992-09-01 Picker International, Inc. Nmr spectroscopy and imaging coil
US5278294A (en) * 1991-05-28 1994-01-11 Hoechst Mitsubishi Kasei Co., Ltd. Monoazo dye having diaminopyridine derivatives
US5330543A (en) * 1991-11-23 1994-07-19 Basf Aktiengesellschaft Thiopheneazo dyes with a coupling component of the diaminopyridine series
US5403363A (en) * 1992-12-07 1995-04-04 Basf Aktiengesellschaft Dye mixtures containing azo dyes having a coupling component from the diaminopyridine series
US5602238A (en) * 1994-08-29 1997-02-11 Ciba-Geigy Corporation Azothiophene dyes containing a 2,4,6-triamino-3-cyanopyridine coupling component
GB2335924A (en) * 1998-03-31 1999-10-06 Zeneca Ltd Dyes and ink jet inks based on 5-([N-substituted-aminoaryl]azo)-4-cyanoisothiazole derivatives
US6187084B1 (en) 1998-03-31 2001-02-13 Zeneca Ltd. Ink compositions
GB2335924B (en) * 1998-03-31 2003-09-03 Zeneca Ltd Dyes and ink compositions comprising 5-azo-isothiazole derivatives
US20050261395A1 (en) * 2002-01-30 2005-11-24 Fuji Photo Film Co., Ltd. Ink composition and inkjet recording method
US20070231204A1 (en) * 2006-03-31 2007-10-04 Searete Llc, A Limited Liability Corporation Of The State Of Delaware Surveying sterilizer methods and systems
US8932535B2 (en) 2006-03-31 2015-01-13 The Invention Science Fund I, Llc Surveying sterilizer methods and systems
US7638090B2 (en) 2006-03-31 2009-12-29 Searete Llc Surveying sterilizer methods and systems
US7754156B2 (en) 2006-03-31 2010-07-13 The Invention Science Fund I, Llc Surveying sterilizer methods and systems
US8114342B2 (en) 2006-03-31 2012-02-14 The Invention Science Fund I, Llc Methods and systems for monitoring sterilization status
US8178042B2 (en) 2006-03-31 2012-05-15 The Invention Science Fund I, Llc Methods and systems for monitoring sterilization status
US8277724B2 (en) 2006-03-31 2012-10-02 The Invention Science Fund I, Llc Sterilization methods and systems
US8758679B2 (en) 2006-03-31 2014-06-24 The Invention Science Fund I, Llc Surveying sterilizer methods and systems
US8992837B2 (en) 2006-03-31 2015-03-31 The Invention Science Fund I, Llc Methods and systems for monitoring sterilization status
US20070286398A1 (en) * 2006-06-07 2007-12-13 Venkatesan Ramamoorthy Voice Recognition Dialing For Alphabetic Phone Numbers

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JPH07108954B2 (en) 1995-11-22
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EP0244740A3 (en) 1989-04-26
JPS62263259A (en) 1987-11-16
EP0244740A2 (en) 1987-11-11

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